Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.4699533C>ACA123097PRNPc.313C>A (p.Pro105Thr)
c.*2C>A (n.*2C>A)
ClinVar dbSNP
20g.4699533C>TCA256788PRNPc.313C>T (p.Pro105Ser)
c.*2C>T (n.*2C>T)
ClinVar dbSNP gnomAD v2 gnomAD v4
20g.4699533C=CA2347156495PRNPc.313C= (p.Pro105=)
c.*2C= (n.*2C=)
dbSNP

Number of alleles fetched